Description:
2+ years of clinical research experience supporting drug trials
Patient facing and entering data entry through various EDC systems
Dealing with patient adverse events, patient screening, and consenting.
Skills:
Clinical research, Clinical trial, Chart review, Patient recruitment, Gcp, Oncology, Pre-screening patients, Regulatory, Data entry
Top Skills Details:
Clinical research,Clinical trial,Chart review,Patient recruitment,Gcp
Additional Skills & Qualifications:
Education: BA/BS required with 2+ years clinical research experience
Experience: Dependent on education as noted above. (Clinical research conducted while in the student environment may be considered on a case-by-case basis). Experience working in health care/health care setting required.
Licensures & Certifications: Successful completion of CITI Program and IATA training required within 3 months of hire. Certification in research through a professional organization required within 1 year of hire.
Experience Level:
Intermediate Level
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.